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79488001: defect van plasmamembraantransport van thyroxine (aandoening)

SNOMED CT Concept\Clinical finding (finding)\...

\Finding of neck region\Finding of thyroid gland\Disorder of thyroid gland\Inherited disorder of thyroid metabolism\Thyroxine transport defect\Thyroxine plasma membrane transport defect
\Finding of neck region\Disorder of neck (disorder)\Disorder of thyroid gland\Inherited disorder of thyroid metabolism\Thyroxine transport defect\Thyroxine plasma membrane transport defect

\Disease\Genetic disease\Hereditary disease\Hereditary metabolic disease\Inborn error of metabolism\Inherited disorder of thyroid metabolism\Thyroxine transport defect\Thyroxine plasma membrane transport defect
\Disease\Genetic disease\Hereditary disease\Hereditary disorder by system\Hereditary disorder of endocrine system (disorder)\Inherited disorder of thyroid metabolism\Thyroxine transport defect\Thyroxine plasma membrane transport defect
\Disease\Disorder of foetus and/or newborn\Congenital disease (disorder)\Inborn error of metabolism\Inherited disorder of thyroid metabolism\Thyroxine transport defect\Thyroxine plasma membrane transport defect
\Disease\Disorder of body system\Hereditary disorder by system\Hereditary disorder of endocrine system (disorder)\Inherited disorder of thyroid metabolism\Thyroxine transport defect\Thyroxine plasma membrane transport defect
\Disease\Disorder of body system\Disorder of endocrine system\Hereditary disorder of endocrine system (disorder)\Inherited disorder of thyroid metabolism\Thyroxine transport defect\Thyroxine plasma membrane transport defect
\Disease\Disorder of body system\Disorder of endocrine system\Disorder of thyroid gland\Inherited disorder of thyroid metabolism\Thyroxine transport defect\Thyroxine plasma membrane transport defect
\Disease\Disorder of neck (disorder)\Disorder of thyroid gland\Inherited disorder of thyroid metabolism\Thyroxine transport defect\Thyroxine plasma membrane transport defect
\Disease\Metabolic disease\Hereditary metabolic disease\Inborn error of metabolism\Inherited disorder of thyroid metabolism\Thyroxine transport defect\Thyroxine plasma membrane transport defect

Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Thyroxine plasma membrane transport defect	Is a	Thyroxine transport defect	true	Inferred relationship	Some
Thyroxine plasma membrane transport defect	Interprets	Biological transport	false	Inferred relationship	Some
Thyroxine plasma membrane transport defect	Finding site	Thyroid structure	false	Inferred relationship	Some
Thyroxine plasma membrane transport defect	Finding site	Cell membrane	false	Inferred relationship	Some
Thyroxine plasma membrane transport defect	Finding site	Entire endocrine gonad (body structure)	false	Inferred relationship	Some
Thyroxine plasma membrane transport defect	Occurrence	Congenital	false	Inferred relationship	Some
Thyroxine plasma membrane transport defect	Occurrence	Congenital	true	Inferred relationship	Some	1
Thyroxine plasma membrane transport defect	Finding site	Thyroid structure	true	Inferred relationship	Some	1

Inbound Relationships

Type

Active

Source

Characteristic

Refinability

Group

This concept is not in any reference sets

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Id	Description	Lang	Type	Status	Case?	Module
131874016	Thyroxine plasma membrane transport defect	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
820543017	Thyroxine plasma membrane transport defect (disorder)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
239791000146117	defect van plasmamembraantransport van thyroxine	nl	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Netherlands NRC maintained module (core metadata concept)
239801000146118	defect van plasmamembraantransport van thyroxine (aandoening)	nl	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Netherlands NRC maintained module (core metadata concept)
249381000146116	verstoord thyroxinetransport door plasmamembraan	nl	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Netherlands NRC maintained module (core metadata concept)